Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
One of the main aims in the management of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency is to achieve adequate suppression of the adrenal cortex with the smallest possible dose of glucocorticoid substitution. To evaluate the administration schedule of current replacem...
Principais autores: | Charmandari, E, Matthews, D, Johnston, A, Brook, C, Hindmarsh, P |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado em: |
2001
|
Registros relacionados
-
Sexual dimorphism in the synchrony of joint growth hormone and cortisol dynamics in children with classic 21-hydroxylase deficiency.
por: Charmandari, E, et al.
Publicado em: (2003) -
Oral hydrocortisone administration in children with classic 21-hydroxylase deficiency leads to more synchronous joint GH and cortisol secretion.
por: Charmandari, E, et al.
Publicado em: (2002) -
Adrenal adenoma secreting 17-hydroxyprogesterone mimicking non-classical 21-hydroxylase deficiency
por: Beata Woźniak, et al.
Publicado em: (2024-11-01) -
First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly in 21-Hydroxylase Deficiency
por: Tomoyo Itonaga, et al.
Publicado em: (2022-01-01) -
Measurement of 17-Hydroxyprogesterone by LCMSMS Improves Newborn Screening for CAH Due to 21-Hydroxylase Deficiency in New Zealand
por: Mark R de Hora, et al.
Publicado em: (2020-01-01)